Iron-Catalyzed Selective Sulfonylation of Alkenes by Sulfonyl Chlorides
Herein, we report an iron-catalyzed approach for the generation of sulfonyl radicals from readily available bulk raw material sulfonyl chlorides and selective sulfonylation of alkenes for the synthesis of β-keto sulfones and vinyl sulfones depending on the reaction conditions. Under mild aerobic oxidation conditions in ethanol, β-keto sulfones were obtained via C(sp<sup>2</sup>)-C bond cleavage, while under argon protection in hexafluoroisopropanol, vinyl sulfones were formed. Mechanism studies reveal that iron salts play the role of hitting two birds with one stone, involving hydrogen atom transfer (HAT) and single-electron transfer (SET) processes.
Authors
- Qiang Bian (ORCID: https://orcid.org/0000-0001-8796-4264)
- Da‐Zhen Xu (ORCID: https://orcid.org/0000-0001-5076-7558)
- Tong‐Tong Zhao
- Ziyu Liu (ORCID: https://orcid.org/0000-0002-8294-2717)
- Keyu Li (ORCID: https://orcid.org/0000-0003-4816-4525)
- Si-Han Zheng
- Shuhan Wang (ORCID: https://orcid.org/0000-0002-6562-3351)
Institutions
- Harbin Institute of Technology (CN)
- Nankai University (CN)
- Beijing Satellite Navigation Center (CN)
- Institute of Navigation (US)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-10-17
- DOI
- https://doi.org/10.1021/acs.joc.5c01566
- Citations
- 1
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.94